Makale
Uluslararası
2024
A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure
HORMONE RESEARCH IN PAEDIATRICS
ss. 306 · 01.10.2024
Atıf için künye
Kizilay, D. O., Karapinar, D. Y., Karadas, N., Karaoglan, M., Akbayram, S., Goksen, D., Gadashova, A., Albayrak, S., Sahinoglu, E. P., KOÇ, C., Unuvar, A., Orbak, Z., Bıçakçı, Z., Akin, L., Albayrak, C., Anik, A., Aral, Y. Z., Cimbek, E. A., Bahadir, A., … Ozen, S. (2024). A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure. HORMONE RESEARCH IN PAEDIATRICS, 306.
BibTeX
@article{kizilay2024-223568,
author = {Kizilay, Deniz Ozalp and Karapinar, Deniz Yilmaz and Karadas, Nihal and Karaoglan, Murat and Akbayram, Sinan and Goksen, Damla and Gadashova, Ayse and Albayrak, Serpil and Sahinoglu, Esra Pekpak and KOÇ, Cansu and Unuvar, Aysegul and Orbak, Zerrin and Bıçakçı, Zafer and Akin, Leyla and Albayrak, Canan and Anik, Ahmet and Aral, Yusuf Ziya and Cimbek, Emine Ayca and Bahadir, Aysenur and Mete, Cem and Ozen, Samim},
title = {A Little Known But Very Common Phenotype in Patients with Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Failure},
journal = {HORMONE RESEARCH IN PAEDIATRICS},
year = {2024},
pages = {306},
issn = {1663-2818},
url = {https://akademik.atauni.edu.tr/yayinlar/223568-a-little-known-but-very-common-phenotype-in-patients-with-congenital-neutropenia}
}